The type I activin receptor ActRIB is required for egg cylinder organization and gastrulation in the mouse

被引:189
作者
Gu, ZY
Nomura, M
Simpson, BB
Lei, H
Feijen, A
van den Eijnden-van Raaij, J
Donahoe, PK
Li, E [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Med, Massachusetts Gen Hosp E,Cardiovasc Res Ctr, Charlestown, MA 02129 USA
[2] Harvard Univ, Sch Med, Dept Surg, Massachusetts Gen Hosp,Pediat Surg Res Lab, Boston, MA 02114 USA
[3] Netherlands Inst Dev Biol, Hubrecht Lab, NL-3584 CT Utrecht, Netherlands
关键词
activin; serine/threonine kinase receptor; gene targeting; mesoderm induction; gastrulation;
D O I
10.1101/gad.12.6.844
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
ActRIB is a type I transmembrane serine/threonine kinase receptor that has been shown to form heteromeric complexes with the type II activin receptors to mediate activin signal. To investigate the function of ActRIB in mammalian development, we generated ActRIB-deficient ES cell lines and mice by gene targeting. Analysis of the ActRIB(-/-) embryos showed that the epiblast and the extraembryonic ectoderm were disorganized, resulting in disruption and developmental arrest of the egg cylinder before gastrulation. To assess the function of ActRIB in mesoderm formation and gastrulation, chimera analysis was conducted. We found that ActRIB(-/-) ES cells injected into wild-type blastocysts were able to contribute to the mesoderm in chimeric embryos, suggesting that ActRIB is not required for mesoderm formation. Primitive streak formation, however, was impaired in chimeras when ActRIB(-/-) cells contributed highly to the epiblast. Further, chimeras generated by injection of wild-type ES cells into ActRIB(-/-) blastocysts formed relatively normal extraembryonic tissues, but the embryo proper developed poorly probably resulting from severe gastrulation defect. These results provide genetic evidence that ActRIB functions in both epiblast and extraembryonic cells to mediate signals that are required for egg cylinder organization and gastrulation.
引用
收藏
页码:844 / 857
页数:14
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